Chr Mutation (hg38) CAid Gene Transcript Linkouts
3g.81578012G>ACA353684737GBE1c.1531C>T (p.Pro511Ser)
c.1408C>T (p.Pro470Ser)
3g.81578012G>CCA353684738GBE1c.1531C>G (p.Pro511Ala)
c.1408C>G (p.Pro470Ala)
3g.81578012G>TCA353684739GBE1c.1531C>A (p.Pro511Thr)
c.1408C>A (p.Pro470Thr)
3g.81578013A>CCA434492477GBE1c.1530T>G (p.Thr510=)
c.1407T>G (p.Thr469=)
3g.81578013A>GCA434492478GBE1c.1530T>C (p.Thr510=)
c.1407T>C (p.Thr469=)
gnomAD v4
3g.81578013A>TCA434492480GBE1c.1530T>A (p.Thr510=)
c.1407T>A (p.Thr469=)
3g.81578014G>ACA2499630GBE1c.1529C>T (p.Thr510Ile)
c.1406C>T (p.Thr469Ile)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.81578014G>CCA353684741GBE1c.1529C>G (p.Thr510Ser)
c.1406C>G (p.Thr469Ser)
3g.81578014G=CA1378698153GBE1c.1529C= (p.Thr510=)
c.1406C= (p.Thr469=)
3g.81578014G>TCA353684740GBE1c.1529C>A (p.Thr510Asn)
c.1406C>A (p.Thr469Asn)
3g.81578015T>ACA2499631GBE1c.1528A>T (p.Thr510Ser)
c.1405A>T (p.Thr469Ser)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
3g.81578015T>CCA353684742GBE1c.1528A>G (p.Thr510Ala)
c.1405A>G (p.Thr469Ala)
3g.81578015T>GCA353684743GBE1c.1528A>C (p.Thr510Pro)
c.1405A>C (p.Thr469Pro)
3g.81578015T=CA1378698154GBE1c.1528A= (p.Thr510=)
c.1405A= (p.Thr469=)
3g.81578016A=CA1378698155GBE1c.1527T= (p.Phe509=)
c.1404T= (p.Phe468=)
3g.81578016A>CCA353684744GBE1c.1527T>G (p.Phe509Leu)
c.1404T>G (p.Phe468Leu)
dbSNP
3g.81578016A>GCA434492489GBE1c.1527T>C (p.Phe509=)
c.1404T>C (p.Phe468=)
3g.81578016A>TCA353684745GBE1c.1527T>A (p.Phe509Leu)
c.1404T>A (p.Phe468Leu)
3g.81578019delCA2666621163GBE1c.1527del (p.Phe509LeufsTer14)
c.1404del (p.Phe468LeufsTer14)
gnomAD v4
3g.81578017A>CCA353684746GBE1c.1526T>G (p.Phe509Cys)
c.1403T>G (p.Phe468Cys)
3g.81578017A>GCA353684747GBE1c.1526T>C (p.Phe509Ser)
c.1403T>C (p.Phe468Ser)
3g.81578017A>TCA353684748GBE1c.1526T>A (p.Phe509Tyr)
c.1403T>A (p.Phe468Tyr)
3g.81578018A=CA1378698156GBE1c.1525T= (p.Phe509=)
c.1402T= (p.Phe468=)
3g.81578018A>CCA353684749GBE1c.1525T>G (p.Phe509Val)
c.1402T>G (p.Phe468Val)
3g.81578018A>GCA2499632GBE1c.1525T>C (p.Phe509Leu)
c.1402T>C (p.Phe468Leu)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.81578018A>TCA353684750GBE1c.1525T>A (p.Phe509Ile)
c.1402T>A (p.Phe468Ile)
3g.81578019A>CCA434492500GBE1c.1524T>G (p.Pro508=)
c.1401T>G (p.Pro467=)
3g.81578019A>GCA434492502GBE1c.1524T>C (p.Pro508=)
c.1401T>C (p.Pro467=)
gnomAD v4
3g.81578019A>TCA434492504GBE1c.1524T>A (p.Pro508=)
c.1401T>A (p.Pro467=)
3g.81578020G>ACA353684753GBE1c.1523C>T (p.Pro508Leu)
c.1400C>T (p.Pro467Leu)
3g.81578020G>CCA353684752GBE1c.1523C>G (p.Pro508Arg)
c.1400C>G (p.Pro467Arg)
3g.81578020G>TCA353684751GBE1c.1523C>A (p.Pro508His)
c.1400C>A (p.Pro467His)
3g.81578021G>ACA353684754GBE1c.1522C>T (p.Pro508Ser)
c.1399C>T (p.Pro467Ser)
3g.81578021G>CCA2499633GBE1c.1522C>G (p.Pro508Ala)
c.1399C>G (p.Pro467Ala)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.81578021G=CA1378698157GBE1c.1522C= (p.Pro508=)
c.1399C= (p.Pro467=)
3g.81578021G>TCA353684755GBE1c.1522C>A (p.Pro508Thr)
c.1399C>A (p.Pro467Thr)
3g.81578022A=CA1378698158GBE1c.1521T= (p.Thr507=)
c.1398T= (p.Thr466=)
3g.81578022A>CCA434492516GBE1c.1521T>G (p.Thr507=)
c.1398T>G (p.Thr466=)
3g.81578022A>GCA207609GBE1c.1521T>C (p.Thr507=)
c.1398T>C (p.Thr466=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.81578022A>TCA434492514GBE1c.1521T>A (p.Thr507=)
c.1398T>A (p.Thr466=)
3g.81578023G>ACA353684756GBE1c.1520C>T (p.Thr507Ile)
c.1397C>T (p.Thr466Ile)
3g.81578023G>CCA353684757GBE1c.1520C>G (p.Thr507Ser)
c.1397C>G (p.Thr466Ser)
3g.81578023G>TCA353684758GBE1c.1520C>A (p.Thr507Asn)
c.1397C>A (p.Thr466Asn)
3g.81578024T>ACA78284839GBE1c.1519A>T (p.Thr507Ser)
c.1396A>T (p.Thr466Ser)
dbSNP gnomAD v4
3g.81578024T>CCA2499634GBE1c.1519A>G (p.Thr507Ala)
c.1396A>G (p.Thr466Ala)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.81578024T>GCA353684759GBE1c.1519A>C (p.Thr507Pro)
c.1396A>C (p.Thr466Pro)
3g.81578024T=CA1378698159GBE1c.1519A= (p.Thr507=)
c.1396A= (p.Thr466=)
3g.81578025C>ACA434492525GBE1c.1518G>T (p.Leu506=)
c.1395G>T (p.Leu465=)
3g.81578025C>GCA434492526GBE1c.1518G>C (p.Leu506=)
c.1395G>C (p.Leu465=)
3g.81578025C>TCA434492528GBE1c.1518G>A (p.Leu506=)
c.1395G>A (p.Leu465=)

Number of alleles fetched